Chemosensory and hyperoxia circuits in C. elegans males influence sperm navigational capacity

PLoS Biol. 2017 Jun 29;15(6):e2002047. doi: 10.1371/journal.pbio.2002047. eCollection 2017 Jun.

Abstract

The sperm's crucial function is to locate and fuse with a mature oocyte. Under laboratory conditions, Caenorhabditis elegans sperm are very efficient at navigating the hermaphrodite reproductive tract and locating oocytes. Here, we identify chemosensory and oxygen-sensing circuits that affect the sperm's navigational capacity. Multiple Serpentine Receptor B (SRB) chemosensory receptors regulate Gα pathways in gustatory sensory neurons that extend cilia through the male nose. SRB signaling is necessary and sufficient in these sensory neurons to influence sperm motility parameters. The neuropeptide Y pathway acts together with SRB-13 to antagonize negative effects of the GCY-35 hyperoxia sensor on spermatogenesis. SRB chemoreceptors are not essential for sperm navigation under low oxygen conditions that C. elegans prefers. In ambient oxygen environments, SRB-13 signaling impacts gene expression during spermatogenesis and the sperm's mitochondria, thereby increasing migration velocity and inhibiting reversals within the hermaphrodite uterus. The SRB-13 transcriptome is highly enriched in genes implicated in pathogen defense, many of which are expressed in diverse tissues. We show that the critical time period for SRB-13 signaling is prior to spermatocyte differentiation. Our results support the model that young C. elegans males sense external environment and oxygen tension, triggering long-lasting downstream signaling events with effects on the sperm's mitochondria and navigational capacity. Environmental exposures early in male life may alter sperm function and fertility.

MeSH terms

  • Aerobiosis
  • Animals
  • Animals, Genetically Modified
  • Caenorhabditis elegans / genetics
  • Caenorhabditis elegans / metabolism
  • Caenorhabditis elegans / physiology*
  • Caenorhabditis elegans Proteins / genetics
  • Caenorhabditis elegans Proteins / metabolism
  • Chemoreceptor Cells / metabolism
  • Chemoreceptor Cells / physiology*
  • Female
  • Hermaphroditic Organisms / genetics
  • Hermaphroditic Organisms / physiology
  • Male
  • Microscopy, Fluorescence
  • Mutation
  • Oocytes / physiology
  • Oxygen / metabolism
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism
  • Sensory Receptor Cells / metabolism
  • Sensory Receptor Cells / physiology*
  • Sperm Motility / genetics
  • Sperm Motility / physiology*
  • Spermatozoa / metabolism
  • Spermatozoa / physiology*
  • Time-Lapse Imaging / methods

Substances

  • Caenorhabditis elegans Proteins
  • Receptors, G-Protein-Coupled
  • Oxygen